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Rhinology|September 24, 2015
IFRD1 gene polymorphisms are associated with nasal polyposis in cystic fibrosis patientsA Baldan, A R Lo Presti, F Belpinati, et al.Human Genetics|July 8, 1998
A quarter of men with idiopathic oligo-azoospermia display chromosomal abnormalities and microdeletions of different types in interval 6 of Yq11L Stuppia, V Gatta, G Calabrese, et al.Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|February 19, 2008
Epidemiology and a novel procedure for large scale analysis of CFTR rearrangements in classic and atypical CF patients: a multicentric Italian studyR Tomaiuolo, F Sangiuolo, C Bombieri, et al.Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|June 21, 2006
Highly preferential association of NonF508del CF mutations with the M470 alleleB M Ciminelli, A Bonizzato, C Bombieri, et al.Human Genetics|April 4, 2000
A new approach for identifying non-pathogenic mutations. An analysis of the cystic fibrosis transmembrane regulator gene in normal individualsC Bombieri, S Giorgi, S Carles, et al.International Archives of Allergy and Immunology|February 13, 2010
The Gene-Environment Interactions in Respiratory Diseases (GEIRD) ProjectR de Marco, S Accordini, L Antonicelli, et al.Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|May 6, 2008
Consensus on the use and interpretation of cystic fibrosis mutation analysis in clinical practiceC Castellani, H Cuppens, M Macek, et al.Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|June 11, 2011
Recommendations for the classification of diseases as CFTR-related disordersC Bombieri, M Claustres, K De Boeck, et al.Pageof 2